5-(2-Pyridyl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90769
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CAS Number 1402240-71-4

science Other reagents with same CAS 1402240-71-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.2002 g/mol
Formula C₁₅H₂₀BNO₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is widely utilized in Suzuki-Miyaura cross-coupling reactions, a pivotal method in organic synthesis for forming carbon-carbon bonds. Its boronic ester group makes it an effective coupling partner with aryl or vinyl halides, enabling the construction of complex molecules, including pharmaceuticals, agrochemicals, and organic materials. Additionally, it serves as a key intermediate in the development of conjugated polymers and small molecules for optoelectronic applications, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its pyridyl and thiophene moieties contribute to electronic properties, making it valuable in designing materials with tailored functionalities.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿53,800.00
inventory 100mg
10-20 days ฿161,400.00

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5-(2-Pyridyl)thiophene-2-boronic acid pinacol ester
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This compound is widely utilized in Suzuki-Miyaura cross-coupling reactions, a pivotal method in organic synthesis for forming carbon-carbon bonds. Its boronic ester group makes it an effective coupling partner with aryl or vinyl halides, enabling the construction of complex molecules, including pharmaceuticals, agrochemicals, and organic materials. Additionally, it serves as a key intermediate in the development of conjugated polymers and small molecules for optoelectronic applications, such as organic

This compound is widely utilized in Suzuki-Miyaura cross-coupling reactions, a pivotal method in organic synthesis for forming carbon-carbon bonds. Its boronic ester group makes it an effective coupling partner with aryl or vinyl halides, enabling the construction of complex molecules, including pharmaceuticals, agrochemicals, and organic materials. Additionally, it serves as a key intermediate in the development of conjugated polymers and small molecules for optoelectronic applications, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its pyridyl and thiophene moieties contribute to electronic properties, making it valuable in designing materials with tailored functionalities.

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